Package 0220-2829-41
Brand: kali bichromicum
Generic: potassium dichromatePackage Facts
Identity
Package NDC
0220-2829-41
Digits Only
0220282941
Product NDC
0220-2829
Description
7 [hp_C] in 1 TUBE (0220-2829-41)
Marketing
Marketing Status
Brand
kali bichromicum
Generic
potassium dichromate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a0e1d88-7fbf-8d1d-e063-6394a90a6398", "openfda": {"unii": ["T4423S18FM"], "spl_set_id": ["860533b3-4126-0cbf-e053-2a91aa0aa699"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "7 [hp_C] in 1 TUBE (0220-2829-41)", "package_ndc": "0220-2829-41", "marketing_start_date": "19830303"}], "brand_name": "Kali bichromicum", "product_id": "0220-2829_0a0e1d88-7fbf-8d1d-e063-6394a90a6398", "dosage_form": "PELLET", "product_ndc": "0220-2829", "generic_name": "POTASSIUM DICHROMATE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kali bichromicum", "active_ingredients": [{"name": "POTASSIUM DICHROMATE", "strength": "7 [hp_C]/7[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}